Preco, Inc.
Oakland, NJ, US
Preco, Inc. appears in FDA device records in Oakland, NJ. FDA records list 4 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 4
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 4 510(k) clearances for Preco, Inc. in 1985.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K853144 | CARD THREE IM TEST ITEM #2035, CARD ONE IM #2036 | KTN | Substantially Equivalent | |
| K852751 | TOLVIDINE RED UNHEATED SERUM SYPHILLIS CARD TEST | GMQ | Substantially Equivalent | |
| K853054 | RF CARD TEST | DHR | Substantially Equivalent | |
| K850604 | PRECO PREGNANCY RAPID CARD TEST, HEM #2028 | JHJ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain